Organoleptic compounds and their use in perfume compositions

ABSTRACT

The present invention is directed to compounds which possess unique organoleptic propertied of the general formula 
     
       
         
         
             
             
         
       
     
     
       
         
         
             
             
         
       
     
                         
wherein R is a hydrogen or selected from the group consisting of C 1 –C 7  moieties and the use of these materials as a fragrance chemical to enhance fragrance in perfumes, toilet waters, colognes, personal products and the like.

FIELD OF THE INVENTION

The present invention relates to new chemical entities and the incorporation and use of the new chemical entities as fragrance materials.

BACKGROUND OF THE INVENTION

There is an ongoing need in the fragrance industry to provide new chemicals to give perfumers and other persons ability to create new fragrances for perfumes, colognes and personal care products. Those with skill in the art appreciate how differences in the chemical structure of the molecule can result in significant differences in the odor, notes and characteristics of a molecule. These variations and the ongoing need to discover and use the new chemicals in the development of new fragrances allows perfumers to apply the new compounds in creating new fragrances.

SUMMARY OF THE INVENTION

The present invention provides novel chemicals, and the use of the chemicals to enhance the fragrance of perfumes, toilet waters, colognes, personal products and the like. In addition, the present invention is directed to the use of the novel chemicals to enhance fragrance in perfumes, toilet waters, colognes, personal products and the like.

More specifically, the present invention is directed to the novel compounds, represented by Formulas I–III set forth below:

wherein R is a hydrogen or selected from the group consisting of C₁–C₇ moieties and the use of these materials as a fragrance chemical to enhance fragrance in perfumes, toilet waters, colognes; personal products and the like.

Another embodiment of the invention is a method for enhancing a perfume composition by incorporating an olfactory acceptable amount of the compounds provided above.

These and other embodiments of the present invention will be apparent by reading the following specification.

DETAILED DESCRIPTION OF THE INVENTION

In Formula I, II and III above, wherein R is a hydrogen or selected from the group consisting of C₁–C₇ moieties and the use of these materials as a fragrance chemical to enhance fragrance in perfumes, toilet waters, colognes, personal products and the like. Representative moieties include alkyl groups such as but not limited to CH₃C₂H₅, C₄H₉C₅H₁₁; CH(CH₃)CH₂CH₂CH₃; CH₂CH(CH₃)CH₂CH₃ and CH₂CH₂CH(CH₃)CH₃; cyclobutyl, cyclopentyl; as well as unsaturated moieties including but not limited to: CH═CHCH₂CH₂CH₃; CH₂CH═CHCH₂CH₃; CH₂CH₂CH═CHCH₃; and CH═C(CH₃)CH₂CH₃. Those with skill in the art will appreciate that the present invention includes various isomers including chiral or optically active isomers, which are contemplated within the scope of the present invention.

In the preferred embodiment of the invention, the novel compounds of the present invention are represented by the following structures:

Those with the skill in the art will appreciate that the compound of Structure I is Cyclopropanepentanol, Alpha, Alpha, Epsilon-Trimethyl-, the compound of Structure II is Cyclopropane, 1-(1,5-Dimethyl-4-Hexenyl)-1-(methoxymethyl)-, the compound of Structure III is Cyclopropanepropanol, alpha, 2-Diethyl-Alpha, 2-Dimethyl.

The compounds of the present invention may be prepared from the corresponding compounds using Yamamoto and Simmon-Smith cyclopropanation reactions by the following sequences:

Those with skill in the art will recognize that some of the compounds of the present invention have a number of chiral centers, thereby providing numerous isomers of the claimed compounds. It is intended herein that the compounds described herein include isomeric mixtures of such compounds, as well as those isomers that may be separated using techniques known to those having skill in the art. Suitable techniques include chromatography such as HPLC, and particularly gel chromatography and solid phase microextraction (“SPME”).

We have discovered that the fragrance compounds of Formulae I–III are well suited for use as a fragrance ingredient.

The use of the compounds of the present invention is widely applicable in current perfumery products, including the preparation of perfumes and colognes, the perfuming of personal care products such as soaps, shower gels, and hair care products as well as air fresheners and cosmetic preparations. The present invention can also be used to perfume cleaning agents, such as, but not limited to detergents, dishwashing materials, scrubbing compositions, window cleaners and the like.

In these preparations, the compounds of the present invention can be used alone or in combination with other perfuming compositions, solvents, adjuvants and the like. The nature and variety of the other ingredients that can also be employed are known to those with skill in the art.

Many types of fragrances can be employed in the present invention, the only limitation being the compatibility with the other components being employed. Suitable fragrances include but are not limited to fruits such as almond, apple, cherry, grape, pear, pineapple, orange, strawberry, raspberry; musk, flower scents such as lavender-like, rose-like, iris-like, carnation-like. Other pleasant scents include herbal and woodland scents derived from pine, spruce and other forest smells. Fragrances may also be derived from various oils, such as essential oils, or from plant materials such as peppermint, spearmint and the like.

A list of suitable fragrances is provided in U.S. Pat. No. 4,534,891, the contents of which are incorporated by reference as if set forth in its entirety. Another source of suitable fragrances is found in Perfumes, Cosmetics and Soaps, Second Edition, edited by W. A. Poucher, 1959. Among the fragrances provided in this treatise are acacia, cassie, chypre, cyclamen, fern, gardenia, hawthorn, heliotrope, honeysuckle, hyacinth, jasmine, lilac, lily, magnolia, mimosa, narcissus, freshly-cut hay, orange blossom, orchid, reseda, sweet pea, trefle, tuberose, vanilla, violet, wallflower, and the like.

Olfactory effective amount is understood to mean the amount of compound in perfume compositions the individual component will contribute to its particular olfactory characteristics, but the olfactory effect of the perfume composition will be the sum of the effects of each of the perfumes or fragrance ingredients. Thus the compounds of the invention can be used to alter the aroma characteristics of the perfume composition, or by modifying the olfactory reaction contributed by another ingredient in the composition. The amount will vary depending on many factors including other ingredients, their relative amounts and the effect that is desired.

The level of compound of the invention employed in the perfumed article varies from about 0.005 to about 10 weight percent, preferably from about 0.5 to about 8 and most preferably from about 1 to about 7 weight percent. In addition to the compounds other agents can be used in conjunction with the fragrance. Well known materials such as surfactants, emulsifiers, polymers to encapsulate the fragrance can also be employed without departing from the scope of the present invention.

Another method of reporting the level of the compounds of the invention in the perfumed composition, i.e., the compounds as a weight percentage of the materials added to impart the desired fragrance. The compounds of the invention can range widely from 0.005 to about 70 weight percent of the perfumed composition, preferably from about 0.1 to about 50 and most preferably from about 0.2 to about 25 weight percent. Those with skill in the art will be able to employ the desired level of the compounds of the invention to provide the desired fragrance and intensity.

The following are provided as specific embodiments of the present invention. Other modifications of this invention will be readily apparent to those skilled in the art. Such modifications are understood to be within the scope of this invention. As used herein all percentages are weight percent unless otherwise noted, ppm is understood to stand for parts per million and g is understood to be grams. IFF as used in the examples is understood to mean International Flavors & Fragrances Inc., New York, N.Y., USA.

EXAMPLE A Preparation of Cyclopropanepentanol, Alpha, Alpha, Epsilon, Trimethyl-

To a dry 500 ml multi-neck round bottom flask fitted with an air stirrer, nitrogen inlet condenser and an addition funnel 62 g of 99% optically pure DH Myrecerol (IFF) and 1000 ml Methylene Chloride were charged in a pot and flame dried and cooled to 10° C. The mixture was heated maintained at 60° C. 800 ml of triisobutyl aluminum was charged in clean dry cannula. The mixture was aged for 7.5 hours. The mixture was quenched with saturated NH₄Cl, aqueous layer separated and the organic layer washed with 200 ml of water. The organic layer was then dried over anhydrous MgSO₄ and the final product was recovered with a 70% yield.

The NMR of the Cyclopropanepentanol, Alpha, Alpha, Epsilon-Trimethyl-is as follows: 0.1 ppm (m, 1H); 0.3–0.5 ppm (m, 3H); 0.7 ppm (s, 1H); 1.0 ppm (d, 3H); 1.2 ppm (s, 7H); 1.3 ppm (m, 1H); 1.4 ppm (m, 5H).

EXAMPLE B Preparation of Cyclopropane 1-(1,5-Dimethyl-4-Hexenyl)-1-(Methoxymethyl)-

To a dry 100 ml multi-neck round bottom flask fitted with an air stirrer, nitrogen inlet condenser and an addition funnel 22 g of ether, 7.5 g of ZnCu, 26.8 g CH₂I₂ and 31 ml of ether were added and stirred. The mixture was heated maintained at 60° C. The mixture was refluxed at 35° C. overnight and the final product was recovered in 70% yield.

The NMR of the cyclopropane 1-(1,5-dimethyl-4-hexenyl)-1-(methoxymethyl)- is as follows: 0.5 ppm (m, 4H); 1.0 ppm (s, 4H); 1.3 ppm (s, 1H); 1.5 ppm (d, 3H); 1.7 ppm (s, 3H); 1.8 ppm (s, 3H); 2.0 ppm (m, 2H); 3.2 ppm (m, 2H); 3.4 ppm (m, 3H) 5.1 ppm (s, 1H).

EXAMPLE C Preparation of Cyclopropanepropanol, Alpha, 2-Diethyl-Alpha, 2-Dimethyl

To a dry 100 ml multi-neck round bottom flask fitted with an air stirrer, nitrogen inlet condenser and an addition funnel 0.22 mole of zinc copper, 0.20 mole of methylene iodide, 200 ml of MTBE and 3 crystals of I₂ were charged and stirred. 0.10 mole of D.H. Ethyl lianlool was added dropwise and the sample was aged at room temperature. Quench with 200 ml of saturated NH4Cl solution, the aqueous phase was separated out and final product was recovered with a 70% yield.

The NMR of the Cyclopropanepropanol, Alpha, 2-Diethyl-Alpha, 2-Dimethyl is as follows: 0.4 ppm (m, 1H); 0.5 ppm (m, 1H); 0.9 ppm (m, 2H); 1.0 ppm (m, 6H); 1.2 ppm (m, 1H); 1.4 ppm (m, 3H); 1.6 ppm (m, 2H); 1.7 ppm (m, 2H); 1.8 ppm (m, 2H) 2.0 ppm (m, 2H); 2.1 ppm (m, 1H).

EXAMPLE D Demonstration Formula (Shower Gel) with Cyclopropanated Dihyro Myrcenol

Aldehyde AA Triplal 15.00 Benzophenone 5.00 Bergamot Oil 100.00 Cardamom Oil 8.00 Dihydro Myrcenol 60.00 Diphenyl Oxide 10.00 Galaxolide 100.00 Geranium Oil 12.00 Hedione 60.00 Hel ional 6.00 Lilial 100.00 Lyral 50.00 Melafleur 12.00 Menthol 37.00 Nerol 45.00 Patchouli Oil 15.00 Peppermint Oil 40.00 Phenyl Ethyl Alcohol 125.00 Spearmint Oil 200.00 Total weight 1000.00 

1. A compound of formula selected from the group consisting of

wherein R is a hydrogen or selected from the group consisting of CH₃, C₂H₅, C₄H₉C₅H₁₁; CH(CH₃)CH₂CH₂CH₃; CH₂CH(CH₃)CH₂CH₃ and CH₂CH₂CH(CH₃)CH₃; cyclobutyl, cyclopentyl; CH═CHCH₂CH₂CH₃; CH₂CH═CHCH₂CH₃; CH₂CH₂CH═CHCH₃; and CH═C(CH₃)CH₂CH₃.
 2. A method of improving, enhancing or modifying a fragrance formulation through the addition of an olfactory acceptable amount of the compound of claim
 1. 3. The method of claim 2 wherein the fragrance is incorporated into a product selected from perfumes, colognes, toilet waters, cosmetic products, personal care products, fabric care products, cleaning products and air fresheners.
 4. The method of claim 3 wherein the cleaning product is selected from the group consisting of detergents, dishwashing compositions, scrubbing compounds and window cleaners.
 5. The method of claim 2, wherein the amount incorporated into a fragrance is from about 0.005 to about 10 weight percent.
 6. The method of claim 2, wherein the amount incorporated into a fragrance is from about 0.5 to about 8 weight percent.
 7. The method of claim 2, wherein the amount of incorporated into a fragrance is from about 1 to about 7 weight percent.
 8. A fragrance formulation containing an olfactory effective amount of the compound of claim
 1. 9. A fragrance product containing a compound of claim
 1. 10. A fragrance compound:


11. A method of improving, enhancing or modifying a fragrance formulation through the addition of an olfactory acceptable amount of the compound of claim
 10. 12. The method of claim 11 wherein the fragrance is incorporated into a product selected from perfumes, colognes, toilet waters, cosmetic products, personal care products, fabric care products, cleaning products and air fresheners.
 13. The method of claim 12 wherein the cleaning product is selected from the group consisting of detergents, dishwashing compositions, scrubbing compounds and window cleaners.
 14. A fragrance formulation containing an olfactory effective amount of the compound of claim
 10. 15. A fragrance product containing a compound of claim
 10. 